Splenic Tuberculosis - A Rare Case Report

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Mona Ahmed Amin Soliman*

Abstract

Splenic tuberculosis (splenic TB) is extremely rare. It is likely to be misdiagnosed as carcinoma of spleen, splenic abscess, lymphoma, or others. The misdiagnosis rate is high if there is no tuberculosis history in other organs. We came across a case of 27 years old immunocompetent female from good socioeconomic background who presented with weight loss and pain in left hypochondriac region. Ultrasonography of abdomen revealed multiple hypo echoic lesions in the spleen. MRI chest and abdomen revealed multiple splenic focal lesions with no contrast enhancement and well defined mass in the posterior mediastinum. Splenectomy was performed and sample was sent for histopathological examination and also microbiological analysis. Microscopic examination revealed splenic tissue with multiple variable sized granulomas showing epithelial cells, lymphocytes and Langhan’s giant cells, the larger one showed wide necrosis with nuclear debris and suppuration together with focal increase in plasma cells. This was consistent with the diagnosis of Mycobacterial infection with MRI finding of only mediastinal lymph node involvement in the lungs.

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Article Details

Amin Soliman, M. A. (2017). Splenic Tuberculosis - A Rare Case Report. Global Journal of Medical and Clinical Case Reports, 4(3), 072–073. https://doi.org/10.17352/2455-5282.000052
Case Reports

Copyright (c) 2017 Amin Soliman MA.

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This work is licensed under a Creative Commons Attribution 4.0 International License.

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